SI-BONE-POC

Silica-based Nanobiomedical Approaches for Treatment of Bone Diseases: Proof-of-Concept

 Coordinatore UNIVERSITATSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITAT MAINZ 

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore Germany [DE]
 Totale costo 161˙560 €
 EC contributo 149˙366 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2012-PoC
 Funding Scheme CSA-SA(POC)
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-01-01   -   2013-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITATSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITAT MAINZ

 Organization address address: Langenbeckstrasse 1
city: Mainz
postcode: 55131

contact info
Titolo: Dr.
Nome: Uta
Cognome: Veith
Email: send email
Telefono: +49 6131 17 9717
Fax: +49 6131 17 9669

DE (Mainz) hostInstitution 149˙366.00

Mappa


 Word cloud

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protein    erc    osteoporosis    expression    bone    patients    silicatein    sponges    silica    biosilica    enzyme    inorganic    grant    idea    material   

 Obiettivo del progetto (Objective)

'Silicatein is a unique enzyme from siliceous sponges that is able to catalyze the formation of an inorganic material, silica or “biosilica” which forms the inorganic skeleton of these sponges. Another exceptional property of this protein is its dual function, as we discovered for the first time in the ERC Advanced Grant “BIOSILICA” (Grant no. 268476): silicatein both (i) acts as an enzyme (biosilica formation) and (ii) exhibits structure-forming/guiding activity. Even more important with regard to the biomedical application of silicatein: the product of the enzymatic reaction, biosilica, is osteogenic and biocompatible and allows the formation of a moldable material – the ideal basis for the potential application in bone healing, as we found. Moreover, we demonstrated that biosilica not only increases the expression of bone morphogenic protein 2 (BMP-2), but also modulates the ratio of expression of two proteins, osteoprotegerin (OPG) and RANKL, that are crucial in pathogenesis of osteoporosis. Hence, biosilica has potential in prophylaxis and therapy of osteoporosis, a major health threat worldwide. Measures to prevent the development of osteoporosis have become increasingly important due to the demographic development in many industrialized countries. Our idea arising from the ERC-funded project is to apply the silica-enzymes fused to a hydroxyapatite-binding protein tag for the formation of bioactive biosilica-based scaffold / nanocomposite materials for bone regeneration and repair in osteoporotic patients and patients with related bone diseases. The proposed project aims at bringing this idea to a pre-demonstration stage by conducting a proof of concept and verifying its innovation potential. The potential commercialization opportunities and the IPR position of this idea will be clarified.'

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